MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION MOBILE COLUMN TRUSYSTEM 7500 U; TABLE, OPERATING-ROOM, ELECTRICAL

Model Number	1730720
Medical Device Problem Code	Key or Button Unresponsive/not Working (4063)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/03/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The investigation is ongoing.All additional and relevant information that is identified following completion of the investigation will be submitted in a final report.
Event or Problem Description
Baxter received a report stating that trusystem 7500 u mobile column had no functions.The table was located at the account and occurred before use.There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Additional Manufacturer Narrative
The baxter technician found the power cord was loose at the integrated plug connection on the column and it needed to be secured.The surgical table is intended for the following use: ¿ patient positioning during surgery, including anesthesia induction and recovery from anesthesia.¿ task-related patient transfer within the operating theatre.¿ for applications in conjunction with intra-operative imaging (e.G.Ct, mrt, x-ray) with specific table components.The technician reset the table and secured the power cord connection to resolve the reported event.Based on this information, no further action is required.Although there was no reported injury with this event, if the report of a total loss of functions were to recur, it could potentially cause serious injury or death.Therefore baxter is reporting this event.

• Brand Name: MOBILE COLUMN TRUSYSTEM 7500 U
• Common Device Name: TABLE, OPERATING-ROOM, ELECTRICAL
• Manufacturer (Section D): BAXTER HEALTHCARE CORPORATION; deerfield IL
• Manufacturer (Section G): BAXTER MEDICAL SYSTEMS GMBH + CO. KG; carl zeiss strasse 7-9; null; saalfeld thuringen 07318 ; GM 07318
• Manufacturer Contact: 25212 w. illinois route 120; round lake, IL 60073 ; 2242702068
• MDR Report Key: 23511614
• Report Number: 3007143268-2025-00078
• Device Sequence Number: 15976974
• Product Code: GDC
• UDI-Device Identifier: 00887761974388
• UDI-Public: (01)00887761974388(11)230124
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 04/14/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Model Number: 1730720
• Device Catalogue Number: 1730720
• Device Lot Number: N/A
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/03/2025
• Supplement Date Received by Manufacturer: 03/27/2026
• Initial Report FDA Received Date: 11/10/2025
• Supplement Report FDA Received Date: 04/14/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/24/2023
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown